スポンサーリンク
Department of Human Genetics, Nagasaki University School of Medicine | 論文
- Isolation and localization of an IDDMK1,2-22-related human endogenous retroviral gene, and identification of a CA repeat marker at its locus
- THE GROWTH HORMONE RECEPTOR GENE MUTATION OF A JAPANESE PATIENT WITH LARON SYNDROME
- Do monochorionic dizygotic twins increase after pregnancy by assisted reproductive technology?
- TWO POLYMORPHIC AvaI AND HhaI SITES IN A DIFFERENTIALLY METHYLATED REGION OF THE HUMAN H19 GENE
- Maternal uniparental disomy for chromosome 14 in a boy with intrauterine growth retardation
- Uniparental disomy and imprinting defects in Japanese patients with Angelman syndrome
- POLYMORPHIC AND TISSUE-SPECIFIC IMPRINTING OF THE HUMAN WILMS TUMOR GENE, WT1
- Genetic Counseling System in Nagasaki University Hospital and Genetic Services in Nagasaki Prefecture-Now and Future
- Special Report A Genetic Counseling System in Nagasaki Prefecture: The Course and Current Status of the Genetic Counseling Unit in Nagasaki University Hospital
- The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32
- Immunocytochemical study of activin type IB receptor (XALK4) in Xenopus oocytes
- Complete hydatidiform mole with coexisting dichorionic diamniotic twins following testicular sperm extraction and intracytoplasmic sperm injection
- Bit-Serial Single Flux Quantum Microprocessor CORE
- Design and Demonstration of Pipelined Circuits Using SFQ Logic(Special Issue on Superconductive Electronics)
- PHYSICAL MAP OF A YAC CONTIG CONTAINING THE REGION OF THE HUMAN GENE (HYRC) COMPLEMENTING HYPER-RADIOSENSITIVITY OF THE SCID MOUSE MUTATION
- Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta
- Iodine Doping in ZnSe in High-Temperature Range by Metalorganic Vapor-Phase Epitaxy
- P1-IS-66 The association between Lactobacillus species and bacterial vaginosis-related bacteria, and bacterial vaginosis scoring in Japanese pregnant women
- A SacII polymorphism in the human ASCL2 (HASH2) gene region
- Familial 15p tetrasomy due to supernumerary marker 15 chromosome associated with Robertsonian translocation between chromosomes 13 and 14